Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Dayse Figueiredo"'
Autor:
Amanda Vasconcelos de Albuquerque, Dayse Figueiredo Ribeiro de Sena, José Lamartine de Andrade Aguiar, Aline Tenório Dourado
Publikováno v:
Mastology. 31
Introduction: Surgery is the most effective treatment for breast cancer; however, several factors can impair the immune system during the perioperative period, including the anesthetic technique. Since metastasis is the leading cause of death, one of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::431b49053160be059a1db79c5acefa05
https://doi.org/10.29289/2594539420210024
https://doi.org/10.29289/2594539420210024
Autor:
Dayse Figueiredo Ribeiro de Sena, Cristal C. Han, Bárbara de Carvalho Freire Santos Moura, Fernando Santa Cruz, Rodrigo Pessoa Cavalcanti Lira, Rodrigo E.A. Coêlho, Flaviano N. Andrade
Publikováno v:
Journal of Glaucoma
Purpose To identify variants in the CYP1B1 gene in northeastern Brazilian patients with primary congenital glaucoma (PCG) and possible genotype-phenotype correlations. Materials and methods This is a cross-sectional observational study of 17 nonrelat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::135c93e84d882c1143212f681be5787d
https://pubmed.ncbi.nlm.nih.gov/30520782
https://pubmed.ncbi.nlm.nih.gov/30520782
Autor:
Jonathan W. Francis, Paul S. Fishman, Robert H. Brown, Christian L. Lorson, Mary P. Remington, Dayse Figueiredo, Johanna C. vanderSpek, Young-Seon Kim, Shinichiro Ikebe, Laura M. Ayala, Philip J. Young
Publikováno v:
Brain Research. 995:84-96
Spinal muscular atrophy (SMA) is a degenerative disorder of spinal motor neurons caused by homozygous mutations in the survival motor neuron (SMN1) gene. Because increased tissue levels of human SMN protein (hSMN) in transgenic mice reduce the motor
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f846e603b3bd9c83d712a946826b2cff
https://doi.org/10.1016/j.brainres.2003.09.063
https://doi.org/10.1016/j.brainres.2003.09.063
Autor:
Dayse Figueiredo, John R. Murphy, Paul S. Fishman, Jonathan W. Francis, Michael A. Schwarzschild, Robert H. Brown, Johanna C. VanderSpek, Mary P. Remington, Orlando Castillo
Publikováno v:
Journal of neurochemistry. 74(6)
This study describes the expression, purification, and characterization of a recombinant fusion toxin, DAB(389)TTC, composed of the catalytic and membrane translocation domains of diphtheria toxin (DAB(389)) linked to the receptor binding fragment of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::392b1b79d51314c13a8cfa3c459dc7af
https://pubmed.ncbi.nlm.nih.gov/10820215
https://pubmed.ncbi.nlm.nih.gov/10820215
Autor:
Jun Wang, Cecilia Santiago-Turla, Janey L. Wiggs, Dayse Figueiredo, Margaret A. Pericak-Vance, Elizabeth A. Del Bono, Karen LaRocque-Abramson, R. Rand Allingham, Jonathan L. Haines, Michael A. Hauser, Kevin Linkroum
Publikováno v:
Investigative Opthalmology & Visual Science. 47:2542
PURPOSE. To determine the distribution of WDR36 sequence variants in a cohort of patients with primary open-angle glaucoma (POAG) in the United States. METHODS. All of the 23 coding exons and flanking introns of the WDR36 gene were sequenced in 118 p
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a684876030262493dc475b494fbac256
https://doi.org/10.1167/iovs.05-1476
https://doi.org/10.1167/iovs.05-1476
Akademický článek
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Publikováno v:
Repositório Institucional da UFPE
Universidade Federal de Pernambuco (UFPE)
instacron:UFPE
Universidade Federal de Pernambuco (UFPE)
instacron:UFPE
O glaucoma congênito primário (GCP) é uma doença genética rara tipicamente diagnosticada durante o primeiro ano de vida como uma causa importante de cegueira infantil em todo o mundo. A prevalência de GCP varia amplamente. Sobre o GCP poder exi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______3056::8e5c4f034151f414d96c90cce0beb541
https://repositorio.ufpe.br/handle/123456789/29964
https://repositorio.ufpe.br/handle/123456789/29964
